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Variant (rsID / SNP)

rs133073

MCHR1

rs133073 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MCHR1. Location: chromosome 22, position 41,075,695. The table records no clinical significance for this variant.

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Reference-table entries

MCHR1Not classified
Variant type
synonymous_variant
Chromosome / position
22:41075695
HGVS
NM_005297.4,c.39C>T,p.Asn13Asn
Allele change
Synonymous_N82N

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.